rs777524402
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;G) | 5 | Familial Hypercholesterolemia |
Make rs777524402(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 11110731 |
Gene | LDLR |
is a | snp |
is | mentioned by |
dbSNP | rs777524402 |
dbSNP (classic) | rs777524402 |
ClinGen | rs777524402 |
ebi | rs777524402 |
HLI | rs777524402 |
Exac | rs777524402 |
Gnomad | rs777524402 |
Varsome | rs777524402 |
LitVar | rs777524402 |
Map | rs777524402 |
PheGenI | rs777524402 |
Biobank | rs777524402 |
1000 genomes | rs777524402 |
hgdp | rs777524402 |
ensembl | rs777524402 |
geneview | rs777524402 |
scholar | rs777524402 |
rs777524402 | |
pharmgkb | rs777524402 |
gwascentral | rs777524402 |
openSNP | rs777524402 |
23andMe | rs777524402 |
SNPshot | rs777524402 |
SNPdbe | rs777524402 |
MSV3d | rs777524402 |
GWAS Ctlg | rs777524402 |
Max Magnitude | 5 |
ClinVar | |
---|---|
Risk | rs777524402(G;G) |
Alt | rs777524402(G;G) |
Reference | Rs777524402(C;C) |
Significance | Probable-Pathogenic |
Disease | Familial hypercholesterolemia |
Variation | info |
Gene | LDLR |
CLNDBN | Familial hypercholesterolemia |
Reversed | 0 |
HGVS | NC_000019.9:g.11221407C>G |
CLNSRC | LDLR @ LOVD |
CLNACC | RCV000238375.1, |